drugset / Trial / NCT00526136

Vernakalant (Oral) Prevention of Atrial Fibrillation Recurrence Post-Conversion Study

NCT00526136

Phase 2 Completed 735 enrolled Advanz Pharma
RandomizedParallel-groupDouble-blindPrevention

Summary

To evaluate the safety, tolerability and efficacy of 3 doses of vernakalant (oral) (150 mg, 300 mg and 500 mg b.i.d.) administered for up to 90 days in subjects with sustained symptomatic atrial fibrillation (AF duration \> 72 hours and \< 6 months).

Timeline

Start
2007-03
Primary completion
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Vernakalant Other / unclassified 150 mg Oral
Subject Vernakalant Other / unclassified 300 mg Oral
Subject Vernakalant Other / unclassified 500 mg Oral

Indications